Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C231/00—Preparation of carboxylic acid amides
  • C07C231/16—Preparation of optical isomers
  • C07C231/20—Preparation of optical isomers by separation of optical isomers
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
  • C07B57/00—Separation of optically-active compounds
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
  • C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
  • C07C237/20—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
  • C07C249/02—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of compounds containing imino groups
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
  • C07C319/26—Separation; Purification; Stabilisation; Use of additives
  • C07C319/28—Separation; Purification

Definitions

• the invention relates to a process for the preparation of optically active amino acid amide whereby a mixture of the L-amino and D-amino acid amides in the presence of an aldehyde and a suitable solvent is converted in whole or in part, by means of an optically active carboxylic acid, into the salt of the amino acid amide and the carboxylic acid, and a portion mainly consisting of one of the diastereoisomers of that salt is separated from the reaction mixture obtained.
• That publication is notably aimed at the preparation of optically pure nitriles, in particular 2-amino-2- (optionally p-substituted) phenyl acetonitrile, using optically pure tartaric acid and a ketone.
• the invention now aims to provide a process with which optically active amino acid amide is obtained with a high yield.
• this is achieved due to the addition of water to the reaction mixture and the quantity of aldehyde amounting to 0.5-4 equivalents relative to the quantity of amino acid amide, whereby the temperature during the conversion is between 70 and 120°C.
• Aldehydes that can be used in the process according to the invention are for instance aromatic aldehydes, such as benzaldehyde, anisaldehyde, o-, p-, or m-nitrobenzaldehyde, o-, p- or m-chlorobenzaldehyde or aliphatic aldehydes, such as isobutyraldehyde or isovaleraldehyde.
• the quantity of aldehyde to be added is 0.5-4.0 equivalents relative to the quantity of amino acid amide, preferably 1-2 equivalents.
• the starting material can also be a mixture of the Schiff bases (formed from aldehydes) of L-amino and D-amino acid amides. In that case it is not strictly necessary to add an extra quantity of aldehyde.
• at least an equimolar quantity of water relative to the quantity of Schiff base should be added. Application of less than an equimolar quantity of water results in a virtually proportional decrease in the yield.
• an efficiency of 99.0% is achieved when using 1.1 equivalents of water in the asymmetric transformation of the Schiff base of phenylglycine amide and benzaldehyde with optically active mandelic acid, against 45.7% when no water is added.
• the quantity of water added in practice will be not be too great, for instance less than 20 equivalents of water relative to the quantity of amino acid amide or the Schiff base thereof.
• the optimum quantity of water to be used varies with the amino acid amide chosen and can be easily determined by a skilled person. In most cases the quantity of water will be between 0.1 and 4 equivalents relative to amino acid amide or the Schiff base thereof, preferably between 0.5 and 3 equivalents.
• the water is added at the beginning of the reaction or in the course of the conversion process.
• the water can be added in any desired manner, for instance as diluent of the reactants or the solvent. Preferably, a sufficient quantity of water is added previously.
• Mixtures of D,L-amino acid amides can be obtained in a manner known per se, for instance by reacting the corresponding ester with ammonia.
• optically active carboxylic acids are used.
• the acid strength (pKa) will be 3 to 5.
• the quantity of optically active carboxylic acid used can be varied within wide limits and will in general be between 0.9 and 1.2 equivalents of carboxylic acid relative to amino acid amide. Preferably, an equivalent quantity of carboxylic acid is used.
• optically active carboxylic acid is determined by, among other things, the specific amino acid amide.
• the melting point of the diastereoisomeric salts should be sufficiently high, in order to enable separation to be effected by means of crystallization.
• the crystal form may also play a role, in connection with ease of filtration and purification by means of a washing liquid.
• phenylglycine amide and p-hydroxyphenylglycine amide for instance, good results are obtained with mandelic acid and 2-pyrrolidone-5-carboxylic acid.
• optically active carboxylic acids can be easily and almost quantitatively recovered through extraction by means of, for instance, methyl-t-butyl ether, methylisobutyl ketone, ethyl acetate, butyl acetate, amyl alcohol or by means of ion exchangers.
• optically active mandelic acid gives the best results as regards the recoverability of the acid and the crystal form obtained.
• the invention also relates to the new intermediate, diastereoisomeric LD and DL salts of L-, resp. D-mandelic acid and D resp. L phenylglycine amide or p-hydroxyphenylglycine amide, the DD and LL-salts of D-resp. L-methionine amide and D- resp. L-2-pyrrolidone-5-carboxylic acid, and the LD and DL-salts of L- resp. D-homophenylalanine amide and D- resp. L-Z-aspartic acid.
• Suitable solvents for the asymmetric transformation are for instance hydrocarbons, such as cyclohexane, heptane and octane, aromatic hydrocarbons, such as toluene, xylene and benzene, ethers, such as methyl tertiary butyl ether, dioxane, tetrahydrofuran and anisole, esters, such as butyl acetate and ethyl acetate, ketones, such as acetone, butanone, methyl isobutyl ketone, carboxylic acids, aldehydes or mixtures of these substances. It will be clear that a solvent should be chosen which does not enter into irreversible chemical reactions with the amino acid amide, the optically active carboxylic acid or the aldehyde.
• the pressure at which the process according to the invention is carried out is not critical and is for instance 0.01-1 MPa.
• the process is preferably carried out at atmospheric pressure.
• the temperature can be varied within wide limits and is in general 70-120°C, preferably 75-100°C.
• the reaction time is mostly 1-8 hours, preferably 1-4 hours.
• the slurry concentration of the diastereoisomeric salts is about 5-30 wt.%, preferably 10-20 wt.%.
• the optically active amino acid amide can be obtained from the separated diastereoisomeric salt by dissolving the salt in a mixture of water and a virtually equimolar quantity of mineral acid, such as hydrochloric acid, sulphuric acid, nitric acid or phosphoric acid, and extracting the optically active carboxylic acid by means of an extraction agent.
• Suitable extraction agents are for instance ethers, alcohols, ketones or esters, such as methyl tertiary butyl ether, methyl isobutyl ketone, ethyl acetate, butyl acetate or amyl alcohol.
• the optically active amino acid amide obtained can be converted into the corresponding amino acid in a known manner by hydrolysis with an excess of diluted mineral acids, such as hydrochloric acid, sulphuric acid, nitric acid or phosphoric acid.
• the hydrolysis is preferably carried out at 60-100°C, in particular at 85-95°C.
• TLC thin-layer chromatography
• Merck 60 F 254 silicagel being used as carrier
• UV (short wave) and ninidrine being used as detection methods.
• the three TLC eluents and the proportions by volume in which they are used are:
• selectivity 50 % + 50 x [ ⁇ ]20 D max. [ ⁇ ]20 D %
• the product obtained contains more than an equivalent quantity of L-2-pyrrolidone-5-carboxylic acid.
• 2.0 g of the diastereoisomeric LL salt is dissolved in 10 ml water, to which subsequently 10 ml 12 N hydrochloric acid is added.
• 1.0 g of the diastereoisomeric LD salt obtained is suspended in 10 ml water, to which subsequently 10 ml 12 N hydrochloric acid is added with stirring.
• the yield of L-phenylglycine after drying amounts to 10.5 g, which corresponds to an efficiency of 92.9%.
• the yield of D-phenylglycine after, successively, neutralization to pH 4 by means of 85 ml 25 wt.% ammonia, cooling to 20°C, filtration, washing on the glass filter with 5 x 30 ml water and drying, amounts to 27.2 g, which corresponds to an efficiency of 90.0%.
• the resulting salt of L-methionine amide and L-2-pyrrolidone-5-carboxylic acid is filtered and washed on the glass filter with 4 x 25 ml ethyl acetate.
• the yield of TLC pure LL salt amounts to 21.2 g, which corresponds to an efficiency of 73.6%.
• 2.8 g (0.01 mole) of the LL salt is dissolved in a mixture of 3 ml water and 2 ml 12 N hydrochloric acid. After addition of 60 ml acetone to this solution, the L-methionine amide.HCl salt is isolated through filtration.
• the yield of TLC pure DL-salt amounts 9.46 g, which corresponds with a efficiency of 53%.
• 5 g (0.01 mole) of the DL-salt is splitted in a mixture of 100 ml water and 3.7 ml 6 N hydrochloric acid, in D-homophenylalanine amide.HCl salt L-Z-aspartic acid, which is extracted with ethylacetate.
• the D-homophenylalanine amide.HCl present in the water layer is hydrolised with 6 N hydrochloric acid at 80°C into D-homophenylalanine.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Analytical Chemistry (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Preparation Of Compounds By Using Micro-Organisms (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Applications Claiming Priority (3)

Publications (2)

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• 1990
  • 1990-02-16 NL NL9000386A patent/NL9000386A/nl not_active Application Discontinuation
• 1991
  • 1991-02-13 KR KR1019910002589A patent/KR0179028B1/ko not_active IP Right Cessation
  • 1991-02-13 HU HU91482A patent/HU212703B/hu not_active IP Right Cessation
  • 1991-02-14 DK DK91200306.8T patent/DK0442584T3/da active
  • 1991-02-14 EP EP91200306A patent/EP0442584B1/en not_active Expired - Lifetime
  • 1991-02-14 AT AT91200306T patent/ATE97125T1/de not_active IP Right Cessation
  • 1991-02-14 ES ES91200306T patent/ES2062660T3/es not_active Expired - Lifetime
  • 1991-02-14 DE DE69100598T patent/DE69100598T2/de not_active Expired - Fee Related
  • 1991-02-15 JP JP3022137A patent/JP2854148B2/ja not_active Expired - Fee Related
  • 1991-02-15 US US07/655,623 patent/US5306826A/en not_active Expired - Lifetime
  • 1991-02-18 CZ CS91418A patent/CZ281203B6/cs not_active IP Right Cessation
• 1994
  • 1994-01-26 SG SG13294A patent/SG13294G/en unknown

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